Surface acoustic wave (SAW)-based formaldehyde gas sensor using bi-layer nanofilms of bacterial cellulose (BC) and polyethyleneimine (PEI) was developed on an ST-cut quartz substrate using sol-gel and spin coating processes. BC nanofilms significantly improve the sensitivity of PEI films to formaldehyde gas, and reduces response and recovery times. The BC films have superfine filamentary and fibrous network structures, which provide a large number of attachment sites for the PEI particles. Measurement results obtained using in situ diffuse reflectance Fourier transform infrared spectroscopy showed that the primary amino groups of PEI strongly adsorb formaldehyde molecules through nucleophilic reactions, thus resulting in a negative frequency shift of the SAW sensor due to the mass loading effect. In addition, experimental results showed that the frequency shifts of the SAW devices are determined by thickness of PEI film, concentration of formaldehyde and relative humidity. The PEI/BC sensor coated with three layers of PEI as the sensing layer showed the optimal sensing performance, which had a frequency shift of 35.6 kHz for 10 ppm formaldehyde gas, measured at room temperature and 30% RH. The sensor also showed good selectivity and stability, with a low limit of detection down to 100 ppb.
It is crucial to develop highly sensitive and selective sensors for ammonia, one of the most common toxic gases which have been widely used in pharmaceutical, chemical and manufacturing industries. In this study, graphene oxide (GO) film was spin-coated onto surfaces of ST-cut quartz surface acoustic wave (SAW) devices with a resonant frequency of 200 MHz for ammonia sensing. The oxygen-containing functional groups (such as hydroxyl and epoxy ones) on the surface of GO film strongly absorb ammonia molecules and thus increase the film stiffness. This is attributed to the main ammonia sensing mechanism of the Love mode SAW devices, which show not only a positive frequency shift of 620 Hz for 500 ppb ammonia gas, but also an excellent selectivity (as compared to other gases such as H2, H2S, CO and NO2) and a good reproducibility, operated at room temperature of 22 o C.
A Love mode surface acoustic wave (SAW) humidity sensor based on bacterial cellulose (BC) coated ST-cut quartz was developed in this study. The BC film is composed of ultrafine interwoven fibers to form a highly porous network, and its surface contains a large amount of hydroxyl groups, which significantly improve the adsorption capability of SAW sensing layer for water molecules. This results in significant mass loading effects and enhanced responsivity of the SAW sensor. The resonant frequency of the sensor changes linearly with RH at lower relative humidity (RH) values (e.g., RH30%), but when RH80%, an exponential increase in frequency shift as a function of RH is obtained due to the enhanced mass loading effect. A frequency shift of 89.8 kHz was measured using a sensor with a BC film with a thickness of 148 nm thick when the RH was increased from 30% to 93%. The frequency of the sensor can be fully shifted back to the original reading when the RH was returned back to 30%, with the response and recovery times of 12 s and 5 s, respectively.The SAW sensor also exhibits good short-term repeatability and long-term stability for humidity sensing.
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An absorption cell containing an ammonium ion-selective electrode has been constructed and used for the determination of mobile nitrogen in steel; this nitrogen is released as ammonia when the steel is heated a t 500 "C in a stream of hydrogen. The cell was used in conjunction with a digital voltmeter and a recorder in order to obtain a continuous record of the progress of the reaction between mobile nitrogen and hydrogen. Results are presented for the determination of 0.0005-0.0108 per cent. of mobile nitrogen in 10 steels using the new equipment and are compared with those obtained by using a spectrophotometric finish based on indophenol blue. The method, with relative standard deviations of 0.0001-0.0003 per cent., is more precise than that with the spectrophotometric finish, with relative standard deviations of 0.0002-0.0006 per cent.
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